Sediment cores retrieved from the Pleistocene Olduvai Basin by the Olduvai Gorge Coring Project (OGCP) provide a high resolution record of tuffs and other volcaniclastic deposits, together with a lacustrine sedimentary record full of paleoenvironmental indicators. Correlating tuffs between the cores and outcrops at Olduvai, where these tuffs are identified at paleoanthropologically important sites, is critical for applying the new paleoenvironmental data to the conditions under which hominins lived. Tuffs and other volcaniclastic deposits from three cores were analyzed for mineral assemblages and glass and mineral major element compositions (feldspar, augite, hornblende, titanomagnetite, and glass where possible) to compare to published geochemical fingerprint data, based on marker tuffs from outcrop equivalents at Olduvai Gorge. In combination with stratigraphic position, these mineralogical and geochemical data were used to correlate between the cores and outcrops, providing direct temporal tie-lines between the cores and sites of paleoanthropological interest. Direct correlations are most certain for Olduvai Bed I, where all major tuff markers from outcrop are identified for one or more of the three core sites, and for the upper part of the underlying Ngorongoro Formation, which includes the Coarse Feldspar Crystal Tuff (CFCT) and Naabi ignimbrites exposed in the oldest Pleistocene exposures of the Western Gorge. Also characterized were the mineral and glass compositions of tuffs and ignimbrites pre-dating the oldest exposed outcrop units, extending our record of explosive events from the Ngorongoro Volcano. While no specific correlations can be confirmed between individual Bed II tuffs in the cores and in outcrops, correlations are possible between the cores themselves (using newly identified tuff compositions), and some potential correlations (non-unique, based on individual mineral phases) between core and outcrop can be used in conjunction with other stratigraphic tools to help constrain the intervals in question.
Figure 3. Stratigraphic section (left) shown with the image (right) of the outcrop highlighting the positions of the three major tuffs. All hominin fossils were found on the surface or in secondarily deposited sediment below the Ileret Tuff (1.52 ± 0.01 Ma). Some of the remains were found above the Lower Ileret Tuff (1.53 ± 0.01 Ma) indicating that the bones must have been buried above it. The large excavation area is visible on the right side of the outcrop and gully; the lower footprint level (Bennett et al., 2009, Dingwall et al., 2013, Hatala et al., 2017) is exposed on the left side of the image. All fragments of KNM-ER 47000 were located on the surface of the lower portion of the outcrop or secondarily buried in sediment eroded from the drainage that extends up the slope from the excavation site toward the right margin of the picture.
Paranthropus boisei was first described in 1959 based on fossils from the Olduvai Gorge and now includes many fossils from Ethiopia to Malawi. Knowledge about its postcranial anatomy has remained elusive because, until recently, no postcranial remains could be reliably attributed to this taxon. Here, we report the first associated hand and upper limb skeleton (KNM-ER 47000) of P. boisei from 1.51 to 1.53 Ma sediments at Ileret, Kenya. While the fossils show a combination of primitive and derived traits, the overall anatomy is characterised by primitive traits that resemble those found in Australopithecus, including an oblique scapular spine, relatively long and curved ulna, lack of third metacarpal styloid process, gracile thumb metacarpal, and curved manual phalanges. Very thick cortical bone throughout the upper limb shows that P. boisei had great upper limb strength, supporting hypotheses that this species spent time climbing trees, although probably to a lesser extent than earlier australopiths. Hand anatomy shows that P. boisei, like earlier australopiths, was capable of the manual dexterity needed to create and use stone tools, but lacked the robust thumb of Homo erectus, which arguably reflects adaptations to the intensification of precision grips and tool use. KNM-ER 47000 provides conclusive evidence that early Pleistocene hominins diverged in postcranial and craniodental anatomy, supporting hypotheses of competitive displacement among these contemporaneous hominins.
Figure 1. Right upper limbs of a modern human (left), chimpanzee (center), and KNM-ER 47000 (right), which preserves lateral portions of the scapula, the distal portion of the humerus, most of the ulna, and most of metacarpals (MCs) 1-3 and proximal phalanges 2-4. KNM-ER 47000 has primitive traits including a gracile thumb MC, lack of MC 3 styloid process, curved phalanges with prominent flexor sheaths, a long and curved ulna, a humerus with thick cortical bone and a prominent brachioradialis flange, and obliquely oriented scapular spine. Derived traits include a relatively long thumb, short manual phalanges, and a lateral scapular glenoid orientation. Scale bar at right is 10 cm.
John Hawks discusses the latest news on the Rising Star Project:
Africa’s richest fossil hominin site has revealed more of its treasure. It’s been a year and a half since scientists announced that a new hominin species, which they called Homo naledi, had been discovered in the Rising Star Cave outside Johannesburg.
Now they say they have established and published the age of the original naledi fossils that garnered global headlines in 2015. Homo naledi lived sometime between 335 and 236 thousand years ago, making it relatively young.
They’ve also announced the discovery of a second chamber in the Rising Star cave system, which contained additional Homo naledi specimens. These include a child and the partial skeleton of an adult male with a well-preserved skull. They have named the skeleton “Neo” – a Sesotho word meaning “a gift”.
The Conversation Africa’s Science Editor Natasha Joseph asked Professor John Hawks, a member of the team, to explain the story behind these finds.
To an ordinary person, 236 000 years is a very long time ago. Why does the team suggest that in fact, Homo naledi is a “young” species?
The course of human evolution has taken the last seven million years since our ancestors diverged from those of chimpanzees and bonobos. The first two-thirds of that long history, called australopiths, were apelike creatures who developed the trick of walking upright on two legs.
Around two million years ago some varieties of hominins took the first real steps in a human direction. They’re the earliest clear members of our genus, Homo, and belong to species like Homo habilis, Homo erectus and Homo rudolfensis.
Homo naledi looks in many ways like these first members of Homo. It’s even more primitive than these species in many ways, and has a smaller brain than any of them. People outside our team who have studied the fossils mostly thought they should be around the same age. A few had the radical idea that H. naledi might have lived more recently, maybe around 900,000 years ago.
Nobody thought that these fossils could actually have come from the same recent time interval when modern humans were evolving, a mere 236 to 335 thousand years ago.
How do you figure out a fossil’s age?
We applied six different methods. The most valuable of these were electron spin resonance (ESR) dating, and uranium-thorium (U-Th) dating. ESR relies on the fact that teeth contain tiny crystals, and the electron energy in these crystals is affected by natural radiation in the ground over long periods of time after fossils are buried.
U-Th relies on the fact that water drips into caves and forms layers of calcite, which contain traces of uranium. The radioactive fraction of uranium decays into thorium slowly over time. So the proportion of thorium compared to uranium gives an estimate of the time since the calcite layers formed. One of these calcite deposits, called a flowstone, formed above the H. naledi fossils in the Dinaledi Chamber. That flowstone helps to establish the minimum age: the fossils must be older than the flowstone above them.
For these two methods, our team engaged two separate labs and asked them to process and analyse samples without talking to each other. Their processes produced the same results. This gives us great confidence that the results are reliable.
What does the discovery of Homo naledi’s age mean for our understanding of human history and evolution?
For at least the past 100 years, anthropologists have assumed that most of the evolution of Homo was a story of progress: brains got bigger over time, technology became more sophisticated and teeth got smaller as people relied more upon cleverness to get better food and prepare it by cooking.
We thought that once culture really got started, our evolution was driven by a feedback loop – better food allowed bigger brains, more clever adaptations, more sophisticated communication. That enabled better technology, which yielded more food, and so on like a snowball rolling downhill.
No other hominin species could compete with this human juggernaut. You would never see more than one form of human in a single part of the world, because the competition would be too intense. Other forms, like Neanderthals, existed within regions of the world apart from the mainstream leading to modern humans in Africa. But even they were basically human with large brains.
That thinking was wrong.
Africa south of the equator is the core of human evolutionary history. That’s where today’s human populations were most genetically diverse, and that diversity is just a small part of what once existed there. Different lineages of archaic humans once lived in this region. Anthropologists have found a few fossil remnants of these archaic populations. They’ve tried to connect those remnants in a straight line. But the genetic evidence suggests that they were much more complex, with deep divisions that occasionally intertwined.
H. naledi shows a lineage that existed for probably more than a million years, maybe two million years, from the time it branched from our family tree up to the last 300,000 years. During all this time, it lived in Africa with archaic lineages of humans, with the ancestors of modern humans, maybe with early modern humans themselves. It’s strikingly different from any of these other human forms, so primitive in many aspects. It represents a lost hominin community within which our species evolved.
I think we have to reexamine much of what we thought we knew about our shared evolutionary past in Africa. We know a lot of information from a few very tiny geographic areas. But the largest parts of the continent are unknown – they have no fossil record at all.
We’re working to change that, and as our team and others make new discoveries, I’m pretty sure we are going to find more lineages that have been hidden to us. H. naledi will not be the last.
The first Homo naledi discoveries were made in the Dinaledi Chamber. What led researchers to the second chamber? And what did you find there?
The Dinaledi Chamber is one of the most significant fossil finds in history. After excavating only a very tiny part of this chamber, the sample of hominin specimens is already larger than any other single assemblage in Africa.
The explorers who first found these bones, Rick Hunter and Steven Tucker, saw what the team was doing when they were excavating in the chamber. The pair realised that they might have seen a similar occurrence in another part of the cave system. The Rising Star system has more than two kilometres of mapped passages underground. In another deep chamber, accessed again through very tight underground squeezes, there were hominin bones exposed on the surface.
Our team first began systematic survey of this chamber, which we named the Lesedi Chamber, in 2014. For two years Marina Elliott led excavations, joined at times by most of the team’s other experienced underground excavators. They were working in a situation where bones are jammed into a tight blind tunnel. Only one excavator can fit at a time, belly-down, feet sticking out. It is an incredibly challenging excavation circumstance.
The most significant discovery is a partial skeleton of H. naledi, with parts of the arms, legs, a lot of the spine and many other pieces, as well as a beautifully complete skull and jaw. We named this skeleton “Neo”. We also recovered fragments of at least one other adult individual, and one child, although we suspect these bones may come from one or two more individuals.
Is there a way for people to view these discoveries in person?
On May 25 – Africa Day – Maropeng at the Cradle of Humankind World Heritage Site outside Johannesburg will open a new exhibit with the discoveries from the Lesedi Chamber and the Dinaledi Chamber together for the first time.
For people outside South Africa, the data from our three-dimensional scans of the new Lesedi fossils are available online.
Anyone can download the 3D models, and people with access to a 3D printer can print their own physical copies of the new fossils, as well as the fossils from the Dinaledi Chamber. It’s a great way for people to see the evidence for themselves.
This evening on the 11th of January 1964, fossil hunter Kamoya Kimeu (1940-Present) was crossing what had been an Early Pleistocene delta to the western side of Lake Natron, Arusha, Tanzania. He was there with a team led by Richard Leakey in search of our earliest ancestors. Barely a few days into the expedition, Kimeu found a hominin mandible, not one of our ancestors, but just an intriguing. It is 1964 and by this time, OH 5, representative of Paranthropus boisei was already gracing the covers of magazines throughout the world. Thought to be the first human that used stone tools for the first time, the Nutcracker Man was not all he was cracked up to be. As more hominin fossils from the Late Pliocene and early Pleistocene began to show, it became more and more clear, that while P. boisei may have been found on an archaeological layer, this is not enough evidence to support a “he’s the first human” hypothesis.
Kimeu had found another representative of P. boisei at Peninj and it was a remarkably complete hominin mandible. The right condyle was missing and so too were the left and right coronoid processes, despite that the fossil had its complete set of teeth and that was particularly key. The teeth showed a great deal of wear to the point that you could see the dentine beneath the enamel. This individual must have eaten alot of sedges and grasses throughout its life to give that sort of result. Grasses and sedges that you could find around deltas like that one that would have entered Lake Natron, when it wasn’t quite as salty. But when exactly did our hominin friend give up its spirit along the shores of the Lake. The stratigraphic layers in the region are like the pages of a picture book, no words, but pictures that can tell better narratives that Twilight could ever even dream of. The mandible was uncovered in a sedimentary layers, comprising the deltas alluvial deposits, sandwiched between two volcanic layers. The volcanic Tuff atop the layer that contained the fossil was previously dated to between 1.6 and 1.4 million years of age, while the basalt below was dated to 1.7 million years of age. You may think that the fossil is probably going to be between 1.7 and 1.4 million years of age, but the team of geologists at the site conducted further analysis at the site to help get a more accurate result. They settled on an age for the mandible of between 1.5 and 1.3 million years of age. Enough time for the ph of a lake to reach beyond 12.
Since the discovery of the Peninj 1 mandible in 1964, another hominin with similar characteristics to P. boisei was found. Paranthropus aethiopicus now joined a trio of hominin species that became the Paranthropines, comprising boisei, robustus (South African hominin) and aethiopicus. Most of what we have collected of these creatures are crania and mandibles, though some postcranial remains have been found. Thankfully the teeth survive well and can tell us a great deal about their diet and the subtle, yet important questions of how they chew their greenery. There was a long drawn out debate over whether these three hominins deserved to live in a separate group – the Paranthropines. Originally, these hominins were classified as robust australopithecines and the palaeoanthropological community decided that a change was needed. The complete anatomy of the Peninj Hominin was never recovered and given that the mandible survived so well, this individual may have fallen to a carnivore in the delta. Below is a summary of the discovery that was made on the 11th of January 1964.